「ethers」の共起表現一覧(1語右で並び替え)
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hosphine) and assists the synthesis of esters, | ethers, amines and thioethers of alcohols. |
Hydrocarbon mixtures are composed of petroleum | ethers and other hydrocarbons. |
They can be easily protected with MTM | ethers and recovered in good yield. |
aliphatic hydrocarbons, ethyl acetate, glycol | ethers, and acetone. |
olvent properties of lower molecular weight of | ethers and alcohols. |
n eliminated completely, however such items as | ethers and potions do appear in the game to be used o |
s alcohols and carboxylic acids into the silyl | ethers and silyl esters, respectively. |
methyl compounds, particularly trifluoromethyl | ethers and trifluoromethyl aromatics, are converted i |
sed with the class of organic compounds called | ethers; and equally, going under its alternative name |
ted him to enter the domain of these superfine | ethers, and become familiar with their mysteries. |
int (175-325°C) than gasoline or the petroleum | ethers, and a lower boiling point than the oils. |
Ethers are slightly polar. | |
Crown | ethers are useful as phase transfer catalysts. |
3,4-Dimethoxybenzyl | ethers are produced in the same ways. |
Glycol | ethers are a group of solvents based on alkyl ethers |
Crown | ethers are not the only macrocyclic ligands that have |
Various silyl | ethers are also popular protecting groups for several |
toxic) mercuric chloride, to which most other | ethers are stable. |
polyphenyl and fluorinated | ethers are the "raw materials" for Nye lubricants. |
Ethers are more polar than alkenes but not as polar a | |
ohols give a substantial amount of alkenes and | ethers as side products. |
unctional molecules becomes possible using MTM | ethers as the protective groups for their hydroxyl gr |
e in the 1960s with the synthesis of the crown | ethers by Charles J. Pedersen. |
Depending on the substituents, some | ethers can be cleaved with a variety of reagents, e.g |
d for the production of perfluorinated amines, | ethers, carboxylic acids, and sulfonic acids. |
In contrast to crown | ethers, cryptands bind the guest ions using both nitr |
Like crown | ethers, cyclen compounds are capable of selectively b |
Unlike most | ethers, does not form peroxides on storage |
mediate in the synthesis of glycerol, glycidyl | ethers, esters and amines. |
f nucleophiles, including enolates, enol silyl | ethers, Grignard reagents, organolithium reagents, al |
Perhaps the most common use of halogenated | ethers has been in anesthesiology. |
MTM | ethers have another advantage. |
the synthesis and binding properties of crown | ethers in a seminal series of papers. |
eophiles and the use of triisopropylsilyl enol | ethers in organic synthesis. |
s are based on a formula containing diglycidyl | ethers, including BADGE. |
suggests that occupational exposure to glycol | ethers is related to low motile sperm count in men, b |
e Selexol solvent is a mixture of the dimethyl | ethers of polyethylene glycol. |
readily available commercially as solutions of | ethers or hydrocarbons; it is not usually prepared in |
The reaction of enolates, enol | ethers, or enol acetates with NBS is the preferred me |
iting the blending of gasoline with "alcohols, | ethers, or other oxygenates." |
Some | ethers rapidly cleave with boron tribromide (even alu |
options of anesthesiologists, but halogenated | ethers remain a mainstay of general anesthesia. |
Schedules I and II to include isomers, esters, | ethers, salts of isomers, esters and ethers, and any |
yl ether has the same properties as some other | ethers, such as volatility, explosive vapors, and the |
xplosions when tert-butyllithium is mixed with | ethers such as diethyl ether, tetrahydrofuran, and gl |
Ethers susceptible to this reaction, a typical exampl | |
reacts faster with t-butyldimethysilyl (TBDMS) | ethers than triisopropylsilyl (TIPS) ethers. |
the para-methoxybenzyl and 3,4-dimethoxybenzyl | ethers, the former are generated by treatment of the |
It also reacts with alcohols to give methyl | ethers, where diazomethane may not. |
are created by the reaction of P4S10 with aryl | ethers which are different from anisole. |
ids (RR'-O+-C-R'R) are prepared by reaction of | ethers with diazo compounds. |
Fatty alcohol polyglycol | ethers with a narrow homolog distribution, which are |
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